Exome Sequencing in Parkinson's Disease

Clinical Genetics - United Kingdom
doi 10.1111/j.1399-0004.2011.01722.x
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Wiley

Related search

Exome Sequencing for the Identification of Mendelian Disease Genes

Erciyes Tip Dergisi
Medicine
2015English

Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease

Arthritis and Rheumatology
RheumatologyAllergyImmunology
2015English

Whole‐exome Sequencing and Immunohistochemistry Findings in Von Hippel–Lindau Disease

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

Whole-Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease

Annals of Clinical and Translational Neurology
NeuroscienceNeurology
2019English

Whole Exome Sequencing in Monogenic Dyslipidemias

Journal of Atherosclerosis and Thrombosis
BiochemistryInternal MedicineCardiovascular MedicineCardiology
2015English

Fronto-Striatal Deficit in Parkinson's Disease During Semantic Event Sequencing

Neurobiology of Aging
AgingGerontologyDevelopmental BiologyGeriatricsNeuroscienceNeurology
2008English

Whole‐exome Sequencing Provides Insights Into Monogenic Disease Prevalence in Northwest Russia

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

Whole Exome Sequencing of Rare Variants in EIF4G1 and VPS35 in Parkinson Disease

Neurology
Neurology
2013English

Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy